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CNNM2

cyclin and CBS domain divalent metal cation transport mediator 2

HCNC Approved Symbol
CNNM2 (HGNC:103)
Genomic Coordinates
10:102,918,294 - 103,090,222 (10q24.32)
Synonyms
ACDP2
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Hypomagnesemia 6, renal
613882AD
Hypomagnesemia, seizures, and impaired intellectual development 1
616418AD; AR

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the CNNM2 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Epilepsy
 1 (100.0%)